GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xyrA in Pseudomonas fluorescens FW300-N1B4

Align D-xylose reductase (EC 1.1.1.307) (characterized)
to candidate Pf1N1B4_5001 Oxidoreductase, aldo/keto reductase family

Query= BRENDA::F2YCN5
         (340 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_5001
          Length = 337

 Score =  130 bits (327), Expect = 5e-35
 Identities = 95/304 (31%), Positives = 151/304 (49%), Gaps = 15/304 (4%)

Query: 28  LGTWAIGGWMWGG-TDDDASIKTIHRAIDLGINIIDTAPAYGRGHAEEVVGKAIKGQRDN 86
           + T  +G  M+G  T  + S++ I +A D GIN IDTA  Y  G +EE+VG+AI  +R  
Sbjct: 13  VSTLTLGTMMFGEQTSTEDSLRIIDKAWDQGINFIDTADVYTNGRSEEIVGEAIASRRQE 72

Query: 87  LIIATKVGLDWTLTPDQSMRRNSSASR--IKKEIEDSLRRLGTDYIDLYQVHWPDPLVPI 144
            ++ATKVG      P   M   S  SR  +   I+ SL RLGTDY+D+Y +H  D   P+
Sbjct: 73  WVLATKVGFG----PVDGMPNRSGLSRKHLFNGIDASLTRLGTDYLDIYYLHREDHNTPL 128

Query: 145 EETATILEALRKEGKIRSIGVSNYSVQQMDEFKKYAEL------AVSQSPYNLFEREIDK 198
           E T + +  L ++GKIR  G+SNY   ++ E  + A+        +SQ  YN+  R+ + 
Sbjct: 129 EVTVSAIGDLIRQGKIRYWGLSNYRGWRIAEVIRIADKLGVDRPVISQPLYNIVNRQAET 188

Query: 199 DILPYAKKNDLVVLGYGALCRGLLSGRMTAD-RAFTGDDLRKTDPKFQKPRFEHYLAAVE 257
           + +  A+   L V+ Y  L RG+LSG+   D          + D +  +  +      + 
Sbjct: 189 EQITAAQNYGLGVVPYSPLARGVLSGKYAPDVTPDANSRAGRQDKRILETEWRVESLRIA 248

Query: 258 ELKKLAKEHYNKSVLALAIRWMLEQGP-TLALWGACKPEQIDGIDEVFGWQISDEDLKQI 316
           +  +   +     ++  AI W+L  G  T A+ G    EQ D   +    +I+ ED   I
Sbjct: 249 QQIQEYTQGRGVGIVEFAIAWVLNNGAVTSAIVGPRTEEQWDAYTKAQAVKITAEDEAFI 308

Query: 317 DAIL 320
           D+++
Sbjct: 309 DSLV 312


Lambda     K      H
   0.317    0.136    0.407 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 291
Number of extensions: 14
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 340
Length of database: 337
Length adjustment: 28
Effective length of query: 312
Effective length of database: 309
Effective search space:    96408
Effective search space used:    96408
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory